SNP Report

Basic Info

Name	rs9557137 dbSNP Ensembl
Location	chr13:99084888 - 99084888(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.302316
Functional Annotation	intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000427887, ENST00000479769); NMD_transcript_variant(ENST00000479769); upstream_gene_variant(ENST00000562781)
No. of Studies	1 (Positive: 1; Negative: 0; Trend: 0)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Detera-Wadleigh, S. D., 2007			FBAT-e P-value = 0.0071 in NIMH1-2, FBAT-e P-value = 0.0877 ...... FBAT-e P-value = 0.0071 in NIMH1-2, FBAT-e P-value = 0.0877 in NIMH3, FBAT-e P-value = 0.1038 in NIMH4 More...	detected evidence of association at the P<0.05 level in the ...... detected evidence of association at the P<0.05 level in the NIMH1-2 More...	Positive

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
DOCK9-AS2	DOCK9 antisense RNA 2 (head to head)	13q32.3	Mapped by Literature SNP
DOCK9	dedicator of cytokinesis 9	13q32.3	1(1/0/0)

SNPs in LD with rs9557137 (count: 0) View in gBrowse (chr13:99084888..99084888 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)